2i3z

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(New page: 200px<br /><applet load="2i3z" size="450" color="white" frame="true" align="right" spinBox="true" caption="2i3z, resolution 2.900&Aring;" /> '''rat DPP-IV with xan...)
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Revision as of 10:01, 21 November 2007

Image:2i3z.jpg

2i3z, resolution 2.900Å

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rat DPP-IV with xanthine mimetic inhibitor #7

Overview

A series of xanthine mimetics containing 5,5 and 5,6 heterocycle fused, imidazoles were synthesized as dipeptidyl peptidase IV inhibitors., Compound 7 is potent (h-DPPIV K(i)=2nM) and exhibits excellent selectivity, and no species specificity against rat and human enzymes. The X-ray, structure confirms that the binding mode of 7 to rat DPPIV is similar to, the parent xanthines.

About this Structure

2I3Z is a Single protein structure of sequence from Rattus norvegicus with LIR as ligand. Active as Dipeptidyl-peptidase IV, with EC number 3.4.14.5 Full crystallographic information is available from OCA.

Reference

Xanthine mimetics as potent dipeptidyl peptidase IV inhibitors., Kurukulasuriya R, Rohde JJ, Szczepankiewicz BG, Basha F, Lai C, Jae HS, Winn M, Stewart KD, Longenecker KL, Lubben TW, Ballaron SJ, Sham HL, von Geldern TW, Bioorg Med Chem Lett. 2006 Dec 15;16(24):6226-30. Epub 2006 Sep 28. PMID:17010607

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